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tert-Butyl ((3-bromopyridin-4-yl)methyl)carbamate

  • CAS No. 1060813-11-7

  • Cat. No. CS-0154384
  • Molecule weight287.15
  • Purity≥98%
  • MDL No.MFCD13189515

*For research and further manufacturing use only, not for direct human use.

tert-Butyl ((3-bromopyridin-4-yl)methyl)carbamate|CS-0154384

Structure of 1060813-11-7

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General Information

  • CAS No. 1060813-11-7
  • Cat. No. CS-0154384
  • Purity ≥98%
  • MDL No. MFCD13189515
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₁₅BrN₂O₂
  • Molecular Weight 287.15
  • Synonym(s) tert-butyl N-[(3-broMopyridin-4-yl)Methyl]carbaMate
  • SMILES CC(C)(OC(NCC1=CC=NC=C1Br)=O)C

Description

tert-Butyl ((3-bromopyridin-4-yl)methyl)carbamate features a brominated pyridine scaffold with a tert-butyl carbamate-protected amine, enabling direct incorporation into diverse synthetic sequences. The electron-deficient pyridine ring facilitates palladium-catalyzed cross-coupling reactions, while the bench-stable carbamate group permits selective deprotection under mild acidic conditions. This combination delivers efficient access to functionalized heterocycles in medicinal chemistry and materials synthesis.

Application

tert-Butyl ((3-bromopyridin-4-yl)methyl)carbamate serves as a versatile building block for the synthesis of pyridine-based pharmaceutical intermediates. The bromo group enables palladium-catalyzed cross-coupling reactions, while the carbamate protects the amine under standard conditions. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient functionalization in medicinal chemistry workflows.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P280-P302+P352

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Computational Chemistry Data

  • TPSA   51.22
  • LogP   2.8688
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   2

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